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Symbol
Name
ID
Isl1
ISL1 transcription factor, LIM/homeodomain
MGI:101791
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Hypertelorism
Disease(s) Associated with ISL1
double outlet right ventricle

Mouse Phenotypes
vision/eye phenotype
increased retina apoptosis
abnormal optic nerve innervation
decreased amacrine cell number
decreased retina ganglion cell number
abnormal retina bipolar cell morphology
abnormal retina ganglion cell morphology
retina ganglion cell degeneration
abnormal optic nerve morphology
optic nerve degeneration
optic nerve hypoplasia
microphthalmia
thin retina inner nuclear layer
thin retina inner plexiform layer
abnormal retina outer plexiform layer morphology
Availability Mouse Genotype
Isl1tm1.1Whk/Isl1tm1.1Whk
Tg(Six3-cre)69Frty/0  (conditional)
*
Isl1tm2Gan/Isl1tm2Gan
Tg(Six3-cre)69Frty/?  (conditional)
Isl1tm1Gan/Isl1tm2Gan
Tg(Six3-cre)69Frty/?  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory